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Clascoterone is safe for the heart, even at high doses.

Systemic retinoids are effective for psoriasis but have side effects; benefits may outweigh risks, especially when reducing cancer risks from other treatments.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Some families have a genetic condition where they are born with irregular scalp defects.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Inflammatory skin conditions are the most common in Brazilian children, with atopic dermatitis being the top issue.

A boy's hair grew back after he stopped using orthodontic headgear that caused temporary hair loss.

Family-based treatment is the best outpatient care for stable teens with anorexia, and more research is needed on medication and treatment effectiveness for young people with eating disorders.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

New 5% minoxidil solution improves scalp hydration, reduces redness, and may be safer for sensitive users.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

Adult female acne treatment should be personalized, considering individual preferences and pregnancy, using various topical and oral medications while managing side effects and resistance.

Dermatologists should screen for and manage psychological issues in patients with skin conditions to improve their quality of life.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Early treatment with immunoglobulin and aspirin reduces heart complications in children with Kawasaki disease.

Alopecia areata may be linked to heart issues.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.